ProfileGDS1065 / 215567_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 32% 41% 25% 33% 40% 44% 25% 38% 39% 31% 39% 39% 37% 32% 35% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 119.832
GSM24653Normal subject 229.241
GSM24654Normal subject 314.425
GSM24655A3243G-MELAS subject 115.633
GSM24656A3243G-MELAS subject 230.940
GSM24657A3243G-MELAS subject 349.544
GSM24658A3243G-MELAS subject 410.825
GSM24659A3243G-PEO subject 123.338
GSM24660A3243G-PEO subject 225.939
GSM24661A3243G-PEO subject 312.431
GSM24662A3243G-PEO subject 424.239
GSM24663mtDNA "Common"-deletion subject 127.739
GSM24664mtDNA "Common"-deletion subject 245.137
GSM24665mtDNA "Common"-deletion subject 328.332
GSM24666mtDNA "Common"-deletion subject 432.435